A negative electrode plate includes a current collector and an active substance layer provided on the current collector, where the active substance layer includes a silicon-based material, and a proportion by mass of element silicon in the active substance layer has a minimum value X1 and a maximum value X2 among different locations of a same area size, where a value of X1/X2 is M, and M≥0.7; and a weight loss rate of the active substance layer under thermogravimetric (TG) analysis within 800° C. has a minimum value Y1 and a maximum value Y2 among different locations of a same area size, where a value of Y1/Y2 is N, and N≥0.7. In this disclosure, the silicon-based material and a binder in the active substance layer are uniformly dispersed, improving C-rate performance and cycling performance of the electrochemical apparatus and reducing swelling of an electrode assembly.

A negative electrode material for a secondary battery includes a matrix containing silicon oxide, a composite oxide of one or more doping elements selected from an alkali metal, an alkaline earth metal, and a post-transition metal, and silicon, or a mixture thereof; and silicon nanoparticles dispersed and embedded in the matrix.

The present disclosure provides a method for forming a solid-state battery. The method includes stacking two or more cell units, where each cell unit is formed by substantially aligning a first electrode and a second electrode, where the first electrode includes one or more first electroactive material layers disposed on or adjacent to one or more surfaces of a releasable substrate and the second electrode includes one or more second electroactive material layers disposed on or adjacent to one or more surfaces of a current collector; disposing an electrolyte layer between exposed surfaces of the first electrode and the second electrode; and removing the releasable substrate to form the cell unit.

A fuel cell assembly includes multiple fuel cells that are electrically coupled. Each fuel cell includes an electrolyte, an anode, and a cathode that can be fabricated from decorated or non-decorated carbon particles. The carbon particles can be produced by a methane dissociating reactor that converts methane into solid carbon and hydrogen. The electrolyte particles form an electrolyte structure that has a pattern of grooves on the anode and cathode facing surfaces. The electrolyte structure is sintered with microwave energy to fuse the adjacent electrolyte particles at contact points. The anode and cathode layers are deposited on opposite sides of the electrolyte and sintered. The anode and cathode layers are then processed to form multiple electrically fuel cells. The anode layers of the fuel cells are electrically coupled with interconnects to cathode layers of the adjacent fuel cells.

Self-charging electrochemical cells, including self-charging batteries that incorporate such self-charging electrochemical cells, the electrochemical cells including a cathode including a cathode active material, an electrolyte including a solvent and a salt dissolved in the solvent, the electrolyte being in contact with the cathode, where the cathode active material is transformed into a discharge product during or after a discharge of the self-charging electrochemical cell and a solubility of the cathode active material in the electrolyte is less than a solubility of the discharge product in the electrolyte.

A method for manufacturing a lithium-ion microbattery having a capacity not exceeding 1 mAh, implementing a method for manufacturing an assembly comprising a porous electrode and a porous separator comprising a porous layer deposited on a substrate having a porosity comprised between 20% and 60% by volume, and pores with an average diameter of less than 50 nm. The separator comprises a porous inorganic layer deposited on the electrode, the porous inorganic layer having a porosity comprised between 20% and 60% by volume, and pores with an average diameter of less than 50 nm.

The cathode material contains the active component, the conductive component and the connecting component. Organic biomaterial is used as the active component, acetylene carbon black is used as the conductive component and polyvinylidene fluoride is used as the connecting component.

A composite cathode active material represented by Li.sub.x(Co.sub.1−wM1.sub.w).sub.yPO.sub.4 (Formula 1) having an olivine structure, wherein a unit-cell volume of the composite cathode active material is in a range of about 283 Å.sup.3 to about 284.6 Å.sup.3. A cathode including the composite cathode active material, and a secondary battery including the composite cathode active material are also disclosed.

In Formula 1, M1 includes i) at least one of Sc, Ti, V, Cr, Cu, or Zn, and optionally at least one of Fe or Ni, and 0.9≤x≤1.1, 0.9≤y≤1.1, and 0<w≤0.3.

This application describes a process for the preparation of carbon-coated particles, where the particles comprise an electrochemically active material. The process comprises the steps of emulsion polymerization, drying and thermally treating the polymer to obtain a nano-layer of carbon on the particles, where the carbon layer comprises fibers and nitrogen-containing polyaromatics have a graphene-like structure. The application also further relates to the particles produced by the method as well as to electrode materials, electrodes and electrochemical cells comprising the particles.

An aluminum battery negative electrode structure includes an aluminum foil and a coating layer. The coating layer is arranged on the aluminum foil. A material of the coating layer includes a high specific surface area carbon material. A specific surface area of the high specific surface area carbon material ranges from 500 m.sup.2/g to 3,000 m.sup.2/g.